Novel cancer therapy extends lives of terminally ill dogs
Published: 19 Jan 2023
Caption: Stock image of a shiba inu and the owner. Copyright: kongsak22
Dogs are humans’ best friends and it is always distressing for dog owners when their beloved pets contract terminal illnesses, with no hope of a cure to treat them safely and effectively.
Canine cancer is the top killer for dogs and when they are diagnosed with late-stage or terminal illness, there are often no treatment options available. In a recent study, however, a novel form of chemoimmunotherapy has proven to be a promising treatment in altering the course of the dogs’ lives.
Scientists at the NUS Centre for Cancer Research (N2CR) Translational Research Programme (TRP) at the Yong Loo Lin School of Medicine, National University of Singapore (NUS Medicine) used stem cell precision engineering technology to treat the cancer-stricken canines.
In the study led by Associate Professor Too Heng-Phon from the N2CR TRP and Department of Biochemistry at NUS Medicine, the team modified Mesenchymal Stem Cells (MSCs), which are able to seek out cancerous tumours. These modified cells carry a potent ‘kill-switch’ (cytosine deaminase) that produces a high, localised concentration of a cancer killing drug (5-fluorouracil) in the tumour environment and subsequently induces anti-cancer immunity. The development of this therapy to treat canine patients leads the team toward a better understanding of cancer treatments, as well as its use in human patients, because helping dogs with naturally occurring cancers provides valuable clues about human cancers.
The technology developed by the NUS Medicine team was first applied on canine patients in Singapore in 2018, in a collaboration with Dr Jean Paul Ly, Chief Executive Officer and Founder, Animal Wellness. The research team thereafter collaborated with more veterinary partners and institutions, delivered the therapy to a total of 65 dogs, and two cats, with conditions such as perianal adenoma, lung metastasis, and sarcoma. The patients first received the precision-engineered MSCs through direct tumour-site injections or through the blood stream, followed by the ingestion of oral pills containing a drug commonly used to treat fungal infection (5-flucytosine), over a few days. After a week, the cycle was repeated for two more weeks before the first course of treatment was completed. The team then monitored the condition of the patients and repeated the course where necessary.
Among the animal patients which received the treatment over a duration ranging from three to eight weeks, 56 showed signs of positive response, including 14 which showed full recovery from the treatment.
Two animal patients remain cancer free, at least 30 months post treatment, while 46 patients showed good quality of life over two to 32 months, with the treatment. Through the course of treatment on all the animal patients involved in the study, there were no significant side effects observed—possibly due to the localised presence of the therapeutic cells which remain within the tumour environment.
There is a massive lag in the development of oncology therapies for animal patients, in contrast to the massive advancements in human cancer treatments. Up until 2009, all animals were treated with generic human chemotherapy medicines on an off-label basis as there were no animal-specific anti-cancer agents approved by the U.S. Food and Drug Administration (FDA).
Dr Lee Yee Lin, Founder and Head Veterinarian, Gentle Oak Veterinary Clinic in Singapore, with whom the research team collaborated and one of the authors of the study, said, “Therapies and advances in allopathic medicine are usually developed primarily for humans, before they are applied to animals. As part of the trials for this study however, dogs with cancer with no other viable treatment options available are the primary receivers of the therapy—and many of them showed promising results with an improvement to their quality of life. Hopefully the therapy can become one of the standard options available to dogs in the near future, so that more patients can benefit from it.”
The stem cell modification therapy differs from other cell and gene therapies that use viruses to introduce genes into cells. Instead of using virus, the modification involves using a chemical carrier, which is safer and faces less regulatory restrictions in the development of the treatment. Compared to other cell and gene therapies, the therapy design has a significantly shorter cycle and much lower costs of production, paving the way for a more accessible and affordable option for cancer patients in future.
Dr Ho Yoon Khei, Senior Research Fellow, N2CR TRP and Department of Biochemistry at NUS Medicine, and first author and lead scientist of the study, said, “Currently, we can develop this therapy for up to 18 human patients every week. Beyond results that have shown to benefit our companion animals, it is our hope to extend the therapy to human patients in the future and improve healthcare outcomes for those who have cancer—especially when they have no treatment options left.”
The research team is working with local and global health institutions to review the therapy’s safety and efficacy for veterinary medicine and discuss plans for clinical trials on human patients in Singapore and the Asia Pacific region. These are expected to begin in 2024.
Read the press release here.
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